유전 상담사

의료 종사자 및 기술직 · 직무 역량 및 필수 스킬 · SOC 29-9092 · 43개 skills

직업 맥락

이 O*NET 작업은 직업을 설명하고 SOC 분류의 맥락을 제공합니다. 목록의 모든 Skill이 모든 작업을 수행한다는 의미는 아닙니다.

Interpret laboratory results and communicate findings to patients or physicians.
Discuss testing options and the associated risks, benefits and limitations with patients and families to assist them in making informed decisions.
Analyze genetic information to identify patients or families at risk for specific disorders or syndromes.

O*NET 작업 설명은 원문 언어(영어)로 표시됩니다. 작업 데이터는 USDOL/ETA의 O*NET® 29.1 Database에서 발췌했으며 CC BY 4.0에 따라 사용됩니다.

대표 출처

이 직업에 분류된 인기 Skills의 제한된 표본으로, GitHub 저장소마다 최대 한 개를 표시합니다. 아래에서 전체 분류 목록을 볼 수 있습니다.

clinpgx-database

davila7/claude-code-templates

Access ClinPGx pharmacogenomics data (successor to PharmGKB). Query gene-drug interactions, CPIC guidelines, allele functions, for precision medicine and genotype-guided dosing decisions.

clinpgx-database

foryourhealth111-pixel/Vibe-Skills

Access ClinPGx pharmacogenomics data (successor to PharmGKB). Query gene-drug interactions, CPIC guidelines, allele functions, for precision medicine and genotype-guided dosing decisions.

clinpgx-database

LeonChaoX/qinyan-academic-skills

Access ClinPGx pharmacogenomics data (successor to PharmGKB). Query gene-drug interactions, CPIC guidelines, allele functions, for precision medicine and genotype-guided dosing decisions.

variant-interpretation

lamm-mit/scienceclaw

ToolUniverse workflow — Variant Interpretation

분류된 모든 Skills

저장소 인기도 또는 최근 출처 활동 순으로 전체 분류 목록을 탐색하세요.

Skill 이름과 설명은 출처 저장소가 제공한 언어를 유지합니다.

필터 (0)

필터

정렬 기준

clinpgx-database

davila7/claude-code-templates

Access ClinPGx pharmacogenomics data (successor to PharmGKB). Query gene-drug interactions, CPIC guidelines, allele functions, for precision medicine and genotype-guided dosing decisions.

clinvar-database

davila7/claude-code-templates

Query NCBI ClinVar for variant clinical significance. Search by gene/position, interpret pathogenicity classifications, access via E-utilities API or FTP, annotate VCFs, for genomic medicine.

clinpgx-database

foryourhealth111-pixel/Vibe-Skills

Access ClinPGx pharmacogenomics data (successor to PharmGKB). Query gene-drug interactions, CPIC guidelines, allele functions, for precision medicine and genotype-guided dosing decisions.

clinpgx-database

LeonChaoX/qinyan-academic-skills

Access ClinPGx pharmacogenomics data (successor to PharmGKB). Query gene-drug interactions, CPIC guidelines, allele functions, for precision medicine and genotype-guided dosing decisions.

variant-interpretation

lamm-mit/scienceclaw

ToolUniverse workflow — Variant Interpretation

family-health-analyzer

分析家族病史、评估遗传风险、识别家庭健康模式、提供个性化预防建议

clinpgx-database

swaruplab/operon

Access ClinPGx pharmacogenomics data (successor to PharmGKB). Query gene-drug interactions, CPIC guidelines, allele functions, for precision medicine and genotype-guided dosing decisions.

genomic-variant-interpretation

awslabs/hcls-agent-skills

Reason about germline and somatic variant classification using ACMG/AMP 2015 and AMP/ASCO/CAP frameworks. Use when the user asks to classify a variant, interpret a VCF annotation, resolve a VUS, apply ACMG criteria, weigh ClinVar evidence, evaluate gnomAD allele frequencies, interpret REVEL/CADD/SpliceAI scores, decide whether PVS1 applies, or assess gene-disease validity before reporting. Triggers include "ACMG", "variant classification", "pathogenic", "likely pathogenic", "VUS", "benign", "ClinVar", "gnomAD", "REVEL", "CADD", "SpliceAI", "PVS1", "loss of function", "nonsense variant", "missense interpretation", "splice variant", "filtering allele frequency", "ClinGen", "somatic variant tier".

interpreting-genetic-testing

CaseMark/skills

Structures genetic test result interpretation with variant classification (ACMG criteria) and clinical actionability. Use when interpreting genetic results, classifying variants, or documenting genetic findings.

OpenVet-Projects/VetClaw

Query OMIA (Online Mendelian Inheritance in Animals) for inherited disorders and traits cataloged across species. The veterinary equivalent of OMIM. Use for genetic disease research and breed predisposition data.

interpreting-genomic-profiling

Structures comprehensive genomic profiling interpretation with actionable mutations and matched therapies. Use when reviewing genomic test results, identifying targeted therapy options, or interpreting NGS panels.

managing-hereditary-cancer-syndromes

Guides hereditary cancer risk assessment with genetic testing criteria and management recommendations. Use when evaluating hereditary cancer risk, ordering genetic testing, or managing high-risk patients.